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EP2125895B1 - Antagoniste du recepteur de facteurs de croissance pour l'allo-immunite de greffe d'organe et l'arteriosclerose - Google Patents

Antagoniste du recepteur de facteurs de croissance pour l'allo-immunite de greffe d'organe et l'arteriosclerose Download PDF

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EP2125895B1
EP2125895B1 EP08750999.8A EP08750999A EP2125895B1 EP 2125895 B1 EP2125895 B1 EP 2125895B1 EP 08750999 A EP08750999 A EP 08750999A EP 2125895 B1 EP2125895 B1 EP 2125895B1
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vegfr
vegf
binding
cells
transplant
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EP2125895A2 (fr
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Kari Alitalo
Karl B. Lemström
Antti I. Nykänen
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Vegenics Pty Ltd
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Vegenics Pty Ltd
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    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/705—Receptors; Cell surface antigens; Cell surface determinants
    • C07K14/71—Receptors; Cell surface antigens; Cell surface determinants for growth factors; for growth regulators
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K39/395—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum
    • A61K39/39533—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum against materials from animals
    • A61K39/3955—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum against materials from animals against proteinaceous materials, e.g. enzymes, hormones, lymphokines
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A61P37/02—Immunomodulators
    • A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
    • C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
    • C07K16/22—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against growth factors ; against growth regulators
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
    • C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
    • C07K16/28—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
    • C07K16/2863—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against receptors for growth factors, growth regulators
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    • C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09—Recombinant DNA-technology
    • C12N15/11—DNA or RNA fragments; Modified forms thereof; Non-coding nucleic acids having a biological activity
    • C12N15/113—Non-coding nucleic acids modulating the expression of genes, e.g. antisense oligonucleotides; Antisense DNA or RNA; Triplex- forming oligonucleotides; Catalytic nucleic acids, e.g. ribozymes; Nucleic acids used in co-suppression or gene silencing
    • C12N15/1136—Non-coding nucleic acids modulating the expression of genes, e.g. antisense oligonucleotides; Antisense DNA or RNA; Triplex- forming oligonucleotides; Catalytic nucleic acids, e.g. ribozymes; Nucleic acids used in co-suppression or gene silencing against growth factors, growth regulators, cytokines, lymphokines or hormones
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    • C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09—Recombinant DNA-technology
    • C12N15/11—DNA or RNA fragments; Modified forms thereof; Non-coding nucleic acids having a biological activity
    • C12N15/113—Non-coding nucleic acids modulating the expression of genes, e.g. antisense oligonucleotides; Antisense DNA or RNA; Triplex- forming oligonucleotides; Catalytic nucleic acids, e.g. ribozymes; Nucleic acids used in co-suppression or gene silencing
    • C12N15/1138—Non-coding nucleic acids modulating the expression of genes, e.g. antisense oligonucleotides; Antisense DNA or RNA; Triplex- forming oligonucleotides; Catalytic nucleic acids, e.g. ribozymes; Nucleic acids used in co-suppression or gene silencing against receptors or cell surface proteins
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K2039/505—Medicinal preparations containing antigens or antibodies comprising antibodies
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/20—Immunoglobulins specific features characterized by taxonomic origin
    • C07K2317/24—Immunoglobulins specific features characterized by taxonomic origin containing regions, domains or residues from different species, e.g. chimeric, humanized or veneered
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/70—Immunoglobulins specific features characterized by effect upon binding to a cell or to an antigen
    • C07K2317/73—Inducing cell death, e.g. apoptosis, necrosis or inhibition of cell proliferation
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/70—Immunoglobulins specific features characterized by effect upon binding to a cell or to an antigen
    • C07K2317/76—Antagonist effect on antigen, e.g. neutralization or inhibition of binding
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2319/00—Fusion polypeptide
    • C07K2319/30—Non-immunoglobulin-derived peptide or protein having an immunoglobulin constant or Fc region, or a fragment thereof, attached thereto
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    • C12N2310/00—Structure or type of the nucleic acid
    • C12N2310/10—Type of nucleic acid
    • C12N2310/11—Antisense
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    • C12N2320/00—Applications; Uses
    • C12N2320/30—Special therapeutic applications

Definitions

  • the method further comprises administering the composition to the organ or the organ donor before the transplant.
  • the inhibitor composition administered at this stage contains a different inhibitor from the composition administered to the recipient.
  • donor cells are implicated in graft rejection, and administering the inhibitors to the donor organ or donor prior to the transplant is contemplated to have beneficial effects during the critical perioperative period.
  • the method further comprises repeated administration of the composition to the recipient.
  • a wide variety of growth factor (including endothelial growth factor) inhibitors are described below in detail for practice of the disclosure. Some of the inhibitors bind to a growth factor or to a receptor, and may be described below as binding constructs.
  • a binding construct may comprise one or more binding uints, as set out in more detail below.
  • Other inhibitors may act indirectly, e.g., at the level of effecting gene or protein expression, or inhibiting downstream signaling by an activated receptor.
  • the level of the protein is reduced to 90%, 80%, 70%, 60%, 50%, 40%, 30%, 20% or less (e.g. 10%, 5%, 1% or less) of the level in the absence of the inhibitor.
  • the compound is a multivalent inhibitor of two or more receptors selected from the group consisting of VEGFR-1, VEGFR-2, VEGFR-3, PDGFR-alpha, and PDGFR-beta.
  • the invention comprises a composition that inhibits ligand binding to VEGFR-2 and inhibits ligand binding to VEGFR-3, for administration to the transplant recipient.
  • immunosuppressive agents include Tacrolimus, Mycophenolic acid, Prednisone, Ciclosporin, Azathioprine, Basiliximab, Cyclosporine, Daclizumab, Muromonab-CD3, Mycophenolate Mofetil, Sirolimus, Methylprednisolone, Atgam, Thymoglobulin, OKT3, Rapamycin, Azathioprine, Cyclosporine, and Interleukin-2 Receptor Antagonist. These agents can be administered singly or in combination.
  • compositions of the disclosure inhibits growth factor stimulation of VEGF receptors and/or PDGF receptors (e.g ., inhibits phosphorylation of the receptors) and thereby inhibits biological responses mediated through the receptors including, but not limited to, PDGFR- and/or VEGFR-mediated angiogenesis and lymphangiogenesis.
  • the polypeptide is part of a binding construct, and the polypeptide is operatively connected with a second polypeptide that binds at least one growth factor selected from the group consisting of VEGF-A, VEGF-B, VEGF-C, VEGF-D, VEGF-E, P1GF, PDGF-A, PDGF-B, PDGF-C, and PDGF-D.
  • the invention involves use of a binding construct comprising: a) a first amino acid sequence at least 90%, preferably 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, 99.5%, or 100% identical, identical to a fragment of the VEGFR-3 extracellular domain, wherein said fragment comprises VEGFR-3 immunoglobulin-like domain 1 amino acid sequence; (b) a second amino acid sequence at least 90% identical to a fragment of the VEGFR-2 extracellular domain, wherein the fragment comprises immunoglobulin-like domain 2 amino acid sequence; and, (c) a third amino acid sequence at least 90%, preferably 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, 99.5%, or 100% identical, identical to a fragment of the VEGFR-1 extracellular domain, wherein the fragment comprises immunoglobulin-like domain 3 amino acid sequence; wherein the first, second, and third amino acid sequences are operatively connected, and wherein the binding construct
  • Binding constructs of the invention include those that bind VEGF/PDGF growth factor monomers, homodimers, and heterodimers.
  • VEGFR-2/KDR/Flk-1 kinase insert domain containing receptor/fetal liver kinase-1, hereinafter "R-2"
  • R-2 kinase insert domain containing receptor/fetal liver kinase-1
  • Both the ligands and the receptors generally exist as dimers, including both homodimers and heterodimers. Such dimers can influence binding.
  • PDGF-AA binds PDGFR- ⁇ / ⁇ .
  • PDGF-AB and PDGF-CC bind PDGFR- ⁇ / ⁇ and PDGFR- ⁇ / ⁇ .
  • PDGFR-BB binds both of the homodimers and the heterodimeric PDGF receptor.
  • PDGF-DD binds PDGF receptor heterodimers and beta receptor homodimers.
  • the linker allows for the formation of a salt bridge or disulfide bond.
  • Linkers may comprise non-naturally occurring amino acids, as well as naturally occurring amino acids that are not naturally incorporated into a polypeptide.
  • the linker comprises a coordination complex between a metal or other ion and various residues from the multiple peptides joined thereby.
  • a particularly preferred water-soluble polymer for use herein is polyethylene glycol (PEG).
  • PEG polyethylene glycol
  • polyethylene glycol is meant to encompass any of the forms of PEG that can be used to derivatize other proteins, such as mono-(C1-C10) alkoxy- or aryloxy-polyethylene glycol.
  • PEG is a linear or branched neutral polyether, available in a broad range of molecular weights, and is soluble in water and most organic solvents. PEG is effective at excluding other polymers or peptides when present in water, primarily through its high dynamic chain mobility and hydrophibic nature, thus creating a water shell or hydration sphere when attached to other proteins or polymer surfaces.
  • PEG is nontoxic, non-immunogenic, and approved by the Food and Drug Administration for internal consumption.
  • Nucleic acid encoding a polypeptide or fragment thereof has been isolated, it is preferably inserted into an amplification and/or expression vector in order to increase the copy number of the gene and/or to express the encoded polypeptide in a suitable host cell and/or to transform cells in a target organism (to express the polypeptide in vivo ).
  • amplification and/or expression vector Numerous commercially available vectors are suitable, though "custom made” vectors may be used as well.
  • the vector is selected to be functional in a particular host cell or host tissue (i.e., for replication and/or expression).
  • the polypeptide or fragment thereof may be amplified/expressed in prokaryotic and/or eukaryotic host cells, e.g,, yeast, insect
  • the vector/expression construct may optionally contain elements such as a 5' flanking sequence, an origin of replication, a transcription termination sequence, a selectable marker sequence, a ribosome binding site, a signal sequence, and one or more intron sequences.
  • the 5' flanking sequence may be homologous (i.e., from the same species and/or strain as the host cell), heterologous (i.e., from a species other than the host cell species or strain), hybrid (i.e., a combination of 5' flanking sequences from more than one source), synthetic, or it may be the native polypeptide 5' flanking sequence.
  • a ribosome binding element commonly called the Shine-Dalgarno sequence (prokaryotes) or the Kozak sequence (eukaryotes), is necessary for translation initiation of mRNA.
  • the element is typically located 3' to the promoter and 5' to the coding sequence of the polypeptide to be synthesized.
  • the Shine-Dalgarno sequence is varied but is typically a polypurine (i.e., having a high A-G content). Many Shine-Dalgarno sequences have been identified, each of which can be readily synthesized using methods set forth above.
  • the strong affinity a ligand for its receptor permits affinity purification of binding constructs, and binding constructs using an affinity matrix comprising a complementary binding partner.
  • Affinity chromatography may be employed, e.g., using either natural binding partners (e.g., a ligand when purifying a binding construct with affinity for the same) or antibodies generated using standard procedures ( e.g., immunizing a mouse, rabbit or other animal with an appropriate polypeptide).
  • the peptides of the present invention may be used to generate such antibodies.
  • Known antibodies or antibodies to known growth factor receptors may be employed when they share an epitope with a targeted binding construct.
  • the described protocols may also be modified and used to produce antibodies against any of the other antigens identified herein as targets for anti-rejection therapy, including but not limited to VEGFR-3, VEGF-C, VEGF-D, the other VEGF growth factors, the PDGF receptors, and the PDGF growth factors.
  • Bispecific antibodies that specifically bind to VEGFR-2 and that specifically bind to other antigens relevant to pathology and/or treatment are produced, isolated, and tested using standard procedures that have been described in the literature. See, e.g., Pluckthun & Pack, Immunotechnology, 3:83-105 (1997 ); Carter et al., J. Hematotherapy, 4: 463-470 (1995 ); Renner & Pfreundschuh, Immunological Reviews, 1995, No. 145, pp. 179-209 ; Pfreundschuh U.S. Patent No. 5,643,759 ; Segal et al., J.
  • Antibody fragments that contain the antigen binding, or idiotype, of the molecule may be generated by known techniques.
  • fragments include, but are not limited to, the F(ab') 2 fragment which may be produced by pepsin digestion of the antibody molecule; the Fab' fragments which may be generated by reducing the disulfide bridges of the F(ab') 2 fragment, and the two Fab' fragments which may be generated by treating the antibody molecule with papain and a reducing agent.
  • a vector comprising an anti-sense nucleotide sequence complementary to at least a part of the Receptor or ligand DNA sequence.
  • a vector comprising an anti-sense sequence may be used to inhibit, or at least mitigate, Receptor or ligand expression.
  • siRNA may be affected by introduction or expression of relatively short homologous dsRNAs. Indeed the use of relatively short homologous dsRNAs may have certain advantages as discussed below.
  • preferred segments of the mRNA target can be identified for design of the siRNA mediating dsRNA oligonucleotides as well as for design of appropriate ribozyme and hammerheadribozyme compositions of the invention (see below).
  • compositions to be used for in vivo administration should be sterile. This is readily accomplished by filtration through sterile filtration membranes, prior to or following lyophilization and reconstitution.
  • Therapeutic compositions generally are placed into a container having a sterile access port, for example, an intravenous solution bag or vial having a stopper pierceable by a hypodermic injection needle.
  • the route of administration of the composition is in accord with known methods, e.g. oral, injection or infusion by intravenous, intraperitoneal, intracerebral, intramuscular, intraocular, intraarterial, or intralesional routes, or by sustained release systems or implantation device.
  • the compositions may be administered continuously by infusion, bolus injection or by implantation device.
  • the composition for parenteral administration ordinarily will be stored in lyophilized form or in solution.
  • sustained-release preparations include semipermeable polymer matrices in the form of shaped articles, e.g. films, or microcapsules.
  • Sustained release matrices include polyesters, hydrogels, polylactides ( U.S. Pat No. 3,773,919 , EP 58,481 ), copolymers of L-glutamic acid and gamma ethyl-L-glutamate ( Sidman, et al., Biopolymers, 22: 547-556 (1983 )), poly (2-hydroxyethyl-methacrylate) ( Langer, et al., J. Biomed. Mater. Res., 15:167-277 (1981 ) and Langer, Chem.
  • Sustained-release compositions also may include liposomes, which can be prepared by any of several methods known in the art (e.g., DE 3,218,121 ; Epstein, et al., Proc. Natl. Acad. Sci. USA, 82:3688-3692 (1985 ); Hwang, et al., Proc. Natl. Acad. Sci. USA, 77:4030-4034 (1980 ); EP 52,322 ; EP 36,676 ; EP 88,046 ; EP 143,949 ).
  • an adenoviral-adenoassociated viral hybrid see, for example, U.S. Patent No. 5,856,152
  • a vaccinia viral or a herpesviral see, for example, U.S. Patent No. 5,879,934 ; U.S. Patent No. 5,849,571 ; U.S. Patent No. 5,830,727 ; U.S. Patent No. 5,661,033 ; U.S. Patent No. 5,328,688
  • Other vectors described herein may also be employed. Replication-deficient viral vectors are specifically contemplated.
  • the expression construct (or indeed the peptides discussed above) may be entrapped in a liposome.
  • Liposomes are vesicular structures characterized by a phospholipid bilayer membrane and an inner aqueous medium. Multilamellar liposomes have multiple lipid layers separated by aqueous medium. They form spontaneously when phospholipids are suspended in an excess of aqueous solution.
  • the expression construct may simply consist of naked recombinant DNA or plasmids. Transfer of the construct may be performed by any of the methods mentioned above that physically or chemically permeabilize the cell membrane. This is applicable particularly for transfer in vitro , however, it may be applied for in vivo use as well.
  • Dubensky, et al., Proc. Nat. Acad. Sci. USA, 81:7529-7533 (1984 ) successfully injected polyomavirus DNA in the form of CaPO 4 precipitates into liver and spleen of adult and newborn mice demonstrating active viral replication and acute infection. Benvenisty and Neshif, Proc. Nat. Acad. Sci.. USA, 83:9551-9555 (1986 ) also demonstrated that direct intraperitoneal injection of CaPO 4 precipitated plasmids results in expression of the transfected genes.
  • Promoters for gene therapy for use in this invention include cytomegalovirus (CMV) promoter/enhancer, long terminal repeat (LTR) of retroviruses, keratin 14 promoter, and ⁇ myosin heavy chain promoter.
  • CMV cytomegalovirus
  • LTR long terminal repeat
  • binding constructs of the present invention when used in a method of treating or preventing a disease, e.g, a graft rejection or arteriosclerosis, may be employed alone, or in combination with other agents. In some embodiments, more than one binding construct may be administered. In some embodiments, a binding construct may be administered together with an immuno suppressive protein, antibody, nucleic acid, or chemotherapeutic agent.
  • immunosuppressant therapy that has some efficacy at reducing transplant rejection alone can be used in combination with the inhibitors of the invention, and such combinations are specifically contemplated as combination therapies of the invention.
  • Exemplary organs that have been transplanted in humans, and for which the methods of the invention are especially applicable include thoracic organs (e.g., heart, lung); abdominal organs (e.g., liver, kidney, pancreas, small intestine).
  • the invention also is applicable for various tissue and cell transplants, including but not limited to pancreatic islet cells, bone marrow cells, cardiac myocytes, blood vessels or vessel fragments, heart valves, bones, and skin.
  • Monitoring of heart transplant recipients for the development of allograft rejection includes non-invasive methods such as intramyocardial electrocardiogram ( Hetzer et al., Ann Thorac Surg 66:1343, 1998 ) and echocardiography, radioisotope techniques, magnetic resonance imaging and immunological methods ( Kemkes et al., J Heart Lung Transplant 11: S221-31, 1992 ).
  • the invention may be more readily understood by reference to the following examples, which are given to illustrate the invention and not in any way to limit its scope.
  • the first several examples describe making and testing inhibitor compounds useful to practicing methods of the invention.
  • the second group of examples describes evidence that the antigens are suitable targets for therapy and/or evidence that such therapy is efficacious.
  • These examples primarily make reference to binding constructs that bind particular growth factors of the VEGF subfamily, but they may also be adapted for use of binding constructs that bind other VEGF subfamily members, as well as for binding constructs that bind PDGF subfamily members.
  • binding constructs comprising other VEFGR receptor fragments, PDGFR receptor fragments, and neuropilin receptor fragments may also be employed in variations of these examples.
  • the chimeric construct R-3D1-R2D2+3/Ig exhibited binding to VEGF-C and not VEGF-A.
  • a second experiment with the R-3D1-R2D2+3/Ig construct showed only weak binding to VEGF-A.
  • the following protocol provides an assay to determine whether a binding construct neutralizes one or more PDGF/VEGF growth factors by preventing the growth factor(s) from stimulating phosphorylation of its receptor.
  • the cells After culturing with the culture mediums described above in the presence or absence of the binding construct, the cells are lysed, immunoprecipitated using anti-receptor (e.g., anti-VEGFR-3) antiserum, and analyzed by Western blotting using anti-phosphotyrosine antibodies.
  • anti-receptor e.g., anti-VEGFR-3 antiserum
  • VEGF-C/D growth factor ligand
  • Binding constructs that reduce or eliminate the ligand-mediated stimulation of receptor phosphorylation are considered neutralizing binding constructs.
  • the ability of the binding construct to block growth factor-mediated cell growth and survival is analyzed relative to the control Tie2 cell line in the presence of IL-3. Growth inhibition in the experimental group relative to the control group demonstrates that the binding construct blocks cell growth, presumably by blocking the binding and cross-linking of receptors by growth factor ligands at the cell surface.
  • VEGFR-3 mAb Neutralizing monoclonal VEGFR-3 antibodies
  • the cardiac allograft spleens were harvested at 5 days after the transplantation to RPMI-1640 medium.
  • the tissue was homogenized with a scalpel and 1x10 6 spleen cells were incubated with FITC- or PE-conjugated antibodies for 15 minutes at room temperature. The cells were then washed twice with PBS and analyzed with a FACScan (Becton Dickinson) flow cytometer.
  • Antibodies used were CD45-FITC (MCA43FT, Serotec), CD68-RPE (MCA341PE, Serotec), OX62-RPE (MCA1029PE, Serotec).
  • IgG1-FITC (MCA43FT, Serotec) and IgG-RPE (MCA1209PE) were used as negative isotype controls.
  • Immunofluorescence double stainings of chronically-rejecting cardiac allografts demonstrated the expression of lymphatic endothelial cell transcription factor Prox-1 in the nucleus of the LYVE-1 + cells, confirming the lymphatic phenotype. This was further supported by the observation that LYVE-1 and rat vascular endothelial cell antigen -1 (RECA-1) were not expressed in same vessels, suggesting that these are markers of lymphatic and vascular EC in the rat, respectively.
  • the proliferation marker Ki67 was infrequently found in LYVE-1 + EC, whereas several Ki67 + LYVE-1 - allograft-infiltrating mononuclear cells were detected outside LYVE-1 + lymphatic vessels.
  • VEGFR-3 Inhibition Decreases Dendritic Cell Recruitment to Spleen
  • VEGFR-3-Ig decreased CCL21 production in the spleen similarly as in the allograft.
  • treatment with VEGFR-3-Ig actually resulted in 1.5 times higher CCL21 mRNA levels in the spleen.
  • VEGFR-3-Ig markedly increased the ratio of spleen-to-allograft CCL21 mRNA from 9:1 to 23:1.
  • VEGFR-3 inhibition did not significantly alter spleen mRNA levels of IL-10 ( Hori et al., Science, 299:1057-1061, 2003 ), IL-6, IFN- ⁇ , TNF- ⁇ , NF- ⁇ B, LT- ⁇ , and LT- ⁇ at 5 days after transplantation. These results suggest that VEGFR-3 inhibition regulates chemokine balance between allograft and secondary lymphoid organs in favour of attenuated immune response.
  • Lymphatic EC in the transplanted heart may originate from recipient BM cells, from recipient non-BM cells or from donor cells. Recently, it was shown that recipient-derived lymphatic endothelial progenitor cells - possibly in the form of macrophages - participate in lymphangiogenesis of human kidney allografts ( Kerjaschki et al., (2006), "Lymphatic endothelial progenitor cells contribute to de novo lymphangiogenesis in human renal transplants," Nat. Med. 12: 230-234 ).
  • macrophages may directly trans-differentiate to lymphatic EC in the inflamed cornea ( Maruyama et al., (2005), "Inflammation-induced lymphangiogenesis in the cornea arises from CD11b-positive macrophages," J. Clin. Invest. 115: 2363-2372 ), and may provide cytokines for the expansion of resident lymphatics ( Kerjaschki, D. (2005), "The crucial role of macrophages in lymphangiogenesis,” J. Clin. Invest. 115: 2316-2319 ).
  • marker gene mice was used as cardiac allograft recipients and found that recipient-derived cells contribute only minimally to the formation of VEGFR-3+ lymphatic vessels in the heterotopically transplanted hearts.
  • the degree of allograft injury may determine whether allograft vascular EC originate from the recipient - as in aortic transplantation - or from the donor - as in cardiac allografts ( Hillebrands et al., (2001), "Origin of neointimal endothelium and alpha-actin-positive smooth muscle cells in transplant arteriosclerosis, J. Clin. Invest., 107: 1411-1422 ). Also, the actual effect of lymphatic endothelium chimerism of transplanted organs on alloimmune responses remains unknown.
  • VEGFR-3 inhibition also had lymphatic EC- and chemokine-mediated effects.
  • both VEGFR-3 and CCL21, a chemokine for CCR7+ APC were co-expressed in allograft lymphatic EC, and VEGFR-3 inhibition decreased allograft CCL21 production.
  • VEGFR-3 in allograft lymphatic EC may regulate the production of CCL21, that may in turn facilitate the movement of APC from the allograft to secondary lymphoid tissue and subsequent alloimmune activation.
  • VEGFR-3 inhibition increased CCL21 production in the spleen.
  • VEGFR-3 inhibition that resulted in decreased CCL21 production did not completely prevent alloimmune responses in recipients receiving suboptimal dose of CsA. Therefore, VEGFR-3 inhibition alone may not completely prevent alloimmune responses in transplant recipients.
  • VEGFR-3 inhibition can be used as induction or adjuvant therapy in the prevention and treatment of acute rejection, in addition to (in combination with) conventional T-cell-targeted immunosuppression. Combination therapy targeting other VEGFR's or PDGFR's or their cognate growth factors also is contemplated.
  • VEGFR-3 inhibition resulted in over two-fold increase in spleen Foxp3 and IL-10 mRNA production. Therefore, VEGFR-3 inhibition may also have beneficial effects on Treg, but further studies are needed to clarify the effect of VEGFR-3 signalling on Tregs.
  • VEGFR-1 and -2 Regulate Inflammation, Myocardial Angiogenesis and Arteriosclerosis in Chronically Rejecting Cardiac Allografts / R1
  • VEGFR-1 Targeting VEGFR-1 with neutralizing antibodies in mice reduced allograft CD11b+ myelomonocyte infiltration and allograft arteriosclerosis.
  • VEGFR-2 inhibition prevented myocardial c-kit+ and CD31+ angiogenesis in the allograft, and decreased allograft inflammation and arteriosclerosis.
  • Mouse chronic rejection heart transplantation model and immunohistochemical stainings were used to identify angiogenesis and progenitor cells in allografts. Marker gene mice and rats, and strain-specific major histocompatibility complex (MHC) class I antibodies, were used to determine whether allograft EC originate from the donor, or from the recipient. Neutralizing antibodies were used to investigate the functional role of VEGFR-1 and VEGFR-2 on mouse cardiac allograft angiogenesis, inflammation, and arteriosclerosis.
  • MHC major histocompatibility complex
  • VEGFR-1 was mainly expressed in allograft ⁇ -SMA+ SMC. In peripheral blood, over 50% of VEGFR-1+ cells coexpressed the myelomonocyte marker CD11b.

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Claims (14)

  1. Composition comprenant un inhibiteur de facteur de croissance endothéliale qui inhibe la stimulation de VEGFR-3 par VEGF-C ou VEGF-D pour utilisation dans l'induction de la tolérance ou l'inhibition du rejet d'une greffe de cellules, de tissu ou d'organe ou l'inhibition de l'artériosclérose chez un receveur de greffe mammifère, l'inhibiteur étant choisi parmi :
    (i) une substance d'anticorps qui immunoréagit avec VEGFR-3 ;
    (ii) un polypeptide de VEGFR-3 soluble qui se lie à VEGF-C ou VEGF-D, le polypeptide de VEGFR-3 soluble comprenant le domaine extracellulaire de VEGFR-3 ou un fragment de celui-ci suffisant pour se lier à VEGF-C ou VEGF-D ;
    (iii) un acide nucléique antisens ou un acide nucléique d'ARN interférence qui inhibe l'expression de VEGFR-3 ;
    (iv) un polypeptide comprenant une séquence d'acides aminés au moins 95 % identique aux acides aminés 138-226, 47-224, 47-314 ou 24-775 de SEQ ID NO: 6 ; et
    (v) un acide nucléique qui code pour un polypeptide de (ii) ou (iv).
  2. Composition selon la revendication 1, dans laquelle l'inhibiteur est une substance d'anticorps choisie parmi un anticorps humanisé, un anticorps humain, un anticorps monoclonal, un fragment d'un anticorps et un polypeptide qui comprend un fragment de liaison d'antigène d'un anticorps.
  3. Composition selon la revendication 1, dans laquelle le polypeptide de VEGFR-3 soluble comprend les premier et deuxième ou les premier, deuxième et troisième domaines de type immunoglobuline du domaine extracellulaire de VEGFR-3.
  4. Composition selon la revendication 1, partie (v), dans laquelle l'acide nucléique est administré dans un vecteur d'expression, facultativement choisi parmi un vecteur viral déficient en réplication tel qu'un rétrovirus, un adénovirus, un virus adéno-associé, un virus de vaccine et un virus de l'herpès.
  5. Composition selon la revendication 4, dans laquelle l'expression du vecteur est inductible par administration d'un agent pharmaceutique exogène ou est induite par un stress endogène chez le receveur de greffe d'organe.
  6. Composition selon la revendication 5, dans laquelle l'expression du vecteur est induite par un stress endogène chez le receveur de greffe, le stress comprenant une élévation d'un marqueur biologique corrélé à un rejet.
  7. Composition selon l'une quelconque des revendications précédentes, la greffe étant une greffe de xénogreffe et la composition étant pour utilisation dans l'induction d'une tolérance pour la xénogreffe ou l'inhibition du rejet de xénogreffe, ou la greffe est une greffe d'allogreffe et la composition est pour utilisation dans l'induction d'une tolérance pour l'allogreffe ou une inhibition d'allo-immunité.
  8. Composition selon l'une quelconque des revendications précédentes, la greffe étant une greffe de cellules ou de tissu, les cellules ou le tissu étant facultativement choisis parmi des cellules souches embryonnaires, des cellules souches pluripotentes, des cellules de précurseurs hématopoïétiques, des cellules de précurseurs neuronaux et des cellules de précurseurs endothéliaux, des cellules d'îlot pancréatique, des myocytes cardiaques, des cellules de moelle osseuse, des cellules endothéliales, et des cellules cutanées.
  9. Composition selon l'une quelconque des revendications 1 à 7, dans laquelle la greffe est un organe ou fragment d'organe capable de remplir des fonctions de l'organe ou capable de régénération en organe.
  10. Composition selon la revendication 9, dans laquelle l'organe ou fragment d'organe transplanté est choisi parmi un coeur, un rein, un poumon, un foie, un intestin, un pancréas, de la peau et des os.
  11. Composition selon l'une quelconque des revendications précédentes, la composition étant administrée selon un ou plusieurs des régimes suivants :
    (i) à l'organe ou au donneur d'organe avant la greffe au receveur ;
    (ii) au receveur de façon répétée ;
    (iii) au receveur de façon peropératoire, par rapport à l'opération de greffe ;
    (iv) au receveur de 1 à 90 jours post-opératoires, par rapport à l'opération de greffe ;
    (v) au receveur de 1 à 60 jours post-opératoires, par rapport à l'opération de greffe ;
    (vi) au receveur de 1 à 30 jours post-opératoires, par rapport à l'opération de greffe ;
    (vii) au receveur de 1 à 15 jours post-opératoires, par rapport à l'opération de greffe ;
    et
    (viii) au receveur après détection de symptômes de rejet de greffe aigu.
  12. Composition selon l'une quelconque des revendications précédentes, le receveur de greffe étant également administré avec au moins l'un de :
    (i) un inhibiteur de VEGFR-1 par un ou plusieurs de ses ligands ;
    (ii) un inhibiteur de VEGFR-2 par un ou plusieurs de ses ligands ;
    (iii) un inhibiteur de PDGFR-alpha par un ou plusieurs de ses ligands ;
    (iv) un inhibiteur de PDGFR-bêta par un ou plusieurs de ses ligands ;
    (v) un agent immunosuppresseur facultativement choisi parmi des corticostéroïdes, des inhibiteurs de calcineurine, des agents antiprolifératifs, des anticorps anti-lymphocyte monoclonaux et des anticorps anti-lymphocyte polyclonaux ; et,
    (vi) un antibiotique ou un agent antifongique.
  13. Composition selon l'une quelconque des revendications précédentes, où :
    (i) il est en outre administré à l'organisme donneur une composition telle que définie dans l'une quelconque des revendications 1 à 3, avant collecte des cellules, tissu ou organe pour greffe au receveur, ou
    (ii) les cellules, tissu ou organe sont en outre mis en contact avec une composition telle que définie dans l'une quelconque des revendications 1 à 3 avant greffe au receveur.
  14. Composition selon l'une quelconque des revendications 1 à 3, les cellules, le tissu ou l'organe étant mis en contact avec la composition avant greffe des cellules, tissu ou organe au receveur.
EP08750999.8A 2007-02-02 2008-02-01 Antagoniste du recepteur de facteurs de croissance pour l'allo-immunite de greffe d'organe et l'arteriosclerose Active EP2125895B1 (fr)

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US20180118804A1 (en) 2018-05-03
US20210395339A1 (en) 2021-12-23
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US20240368248A1 (en) 2024-11-07

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